To evaluate whether angiogenic factors are of clinical relevance to actual
human pancreatic cancers, we studied the intratumoral microvessel density (
IMD), and PD-ECGF, VEGF protein expression in 40 pancreatic cancers using i
mmunohistochemistry. We also investigated PD-ECGF and VEGF gene expression
using reverse transcriptase-PCR (RT-PCR). Of the 40 pancreatic cancers stud
ied, 30 carcinomas (75.0%) were evaluated to be PD-ECGF-positive and 10 car
cinomas (25.0%) were determined to be PD-ECGF-negative. In contrast, 27 car
cinomas (67.5%) were evaluated to be VEGF-positive, whereas 13 carcinomas (
32.5%) were VEGF-negative. VEGF gene expression was moderately associated w
ith an increase in the IMD (r(2) = 0.181, P = 0.006), but no significant re
lationship was found between PD-ECGF gene expression and the IMD (r(2) = 0.
093, P = 0.059), However, tumours with positive expression for both PD-ECGF
and VEGF had a higher IMD (P = 0.027), The results of the immunohistochemi
stry agreed well with the results of the quantitative RT-PCR, The median su
rvival time of the hypervascular group was significantly shorter than that
of the hypovascular group (P < 0.0001). In comparing the survival according
to PD-ECGF and VEGF gene expression, the median survival time of the patie
nts with positive PD-ECGF expression was significantly shorter than those w
ith negative PD-ECGF expression (P = 0.040). Furthermore, the median surviv
al time of the patients with positive VEGF expression was significantly sho
rter than those with negative VEGF expression (P = 0.048), However, the Cox
multivariate analysis indicated that the IMD and VEGF expression were inde
pendent prognostic factors of the various clinicopathologic variables in pa
ncreatic cancer patients (P = 0.0021 and P = 0.0443, respectively).